Phenylboronic acid pinacol ester
98%
- Product Code: 91219
Alias:
2-Phenyl-4,4,5,5-tetramethyl-1,3,2-dioxaborinane
CAS:
24388-23-6
| Molecular Weight: | 204.07 g./mol | Molecular Formula: | C₁₂H₁₇BO₂ |
|---|---|---|---|
| EC Number: | MDL Number: | MFCD00966985 | |
| Melting Point: | 27-31 °C(lit.) | Boiling Point: | |
| Density: | Storage Condition: | room temperature |
Product Description:
Phenylboronic acid pinacol ester is widely used in organic synthesis, particularly in Suzuki-Miyaura cross-coupling reactions. This reaction is essential for forming carbon-carbon bonds, making it valuable in the production of pharmaceuticals, agrochemicals, and advanced materials. It serves as a stable and easily handled precursor to phenylboronic acid, which is reactive in these coupling processes. Additionally, it is employed in the synthesis of complex organic molecules, including natural products and polymers, due to its compatibility with various functional groups. Its stability under normal conditions makes it a preferred choice in laboratory and industrial settings for efficient and selective chemical transformations.
Product Specification:
| Test | Specification |
|---|---|
| PURITY GC | 98 100% |
| MELTING POINT | 27-31 |
| APPEARANCE | WHITE TO YELLOW SOLID OR LIQUID |
| INFRARED SPECTRUM | Conforms to Structure |
| NOTE: | This product is low melting point solid,may change state in different environments (solid, liquid or semi-solid) |
Sizes / Availability / Pricing:
| Size (g) | Availability | Price | Quantity |
|---|---|---|---|
| 5.000 | 10-20 days | ฿410.00 |
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| 25.000 | 10-20 days | ฿1,360.00 |
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| 100.000 | 10-20 days | ฿4,290.00 |
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Phenylboronic acid pinacol ester
Phenylboronic acid pinacol ester is widely used in organic synthesis, particularly in Suzuki-Miyaura cross-coupling reactions. This reaction is essential for forming carbon-carbon bonds, making it valuable in the production of pharmaceuticals, agrochemicals, and advanced materials. It serves as a stable and easily handled precursor to phenylboronic acid, which is reactive in these coupling processes. Additionally, it is employed in the synthesis of complex organic molecules, including natural products and polymers, due to its compatibility with various functional groups. Its stability under normal conditions makes it a preferred choice in laboratory and industrial settings for efficient and selective chemical transformations.
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